Argentum 0.4% Adult

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2024-01-30
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:25:55

Label at a glance#

ProductArgentum 0.4% Adult

Active ingredientSILVER

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR RECTAL USE.

DOSAGE & ADMINISTRATION SECTION

Insert 1 suppository as needed.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: 100 gm contains:
4 gm Argentum met. (Silver) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Cocoa butter, Micronized silica gel

"prepared using rhythmical processes"

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.

KEEP REFRIGERATED OR STORE IN COOL, DRY PLACE.

REFRIGERATE TO RESOLIDIFY.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Argentum 0.4 Adult Supp.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1371-1	Argentum 0.4% Adult	10 in 1 BOX	SUPPOSITORY	10		1
48951-1371-1	Argentum 0.4% Adult	2 g in 1 BLISTER PACK	SUPPOSITORY	2		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1371	ARGENTUM 0.4% ADULT SUPPOSITORY [URIEL PHARMACY INC.]	1	2 package rows	20240131_102ecba5-a2b9-2111-e063-6394a90aac20.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Argentum 0.4% Adult
COCOA BUTTER
SILICON DIOXIDE
SILVER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-1371	48951-1371-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
COCOA BUTTER	512OYT1CRR	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
SILVER	3M4G523W1G	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
102ecba5-a2b8-2111-e063-6394a90aac20			102ecba5-a2b9-2111-e063-6394a90aac20	2024-01-30	Warnings	Exact identifier spl id: 102ecba5-a2b8-2111-e063-6394a90aac20 spl set id: 102ecba5-a2b9-2111-e063-6394a90aac20

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.